Variant report

Variant	nsv1054995
Chromosome Location	chr14:38078027-38138176
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:340)
CpG islands
(count:1099)
Chromatin interactive
region (count:45)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:38095040-38095946	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:38124733-38125097	K562	blood:	n/a	n/a
3	ARID3A	chr14:38077854-38078044	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:38119574-38120199	HepG2	liver:	n/a	n/a
5	BACH1	chr14:38124641-38125044	H1-hESC	embryonic stem cell:	n/a	chr14:38124642-38124656 chr14:38124835-38124849
6	BACH1	chr14:38124640-38125109	K562	blood:	n/a	chr14:38124642-38124656 chr14:38124835-38124849
7	BACH1	chr14:38091310-38092347	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr14:38091819-38092100	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr14:38124669-38124869	K562	blood:	n/a	n/a
10	CEBPB	chr14:38079980-38080100	HepG2	liver:	n/a	chr14:38080019-38080030
11	CEBPB	chr14:38137899-38138291	IMR90	lung:	n/a	chr14:38138090-38138103
12	CEBPB	chr14:38081883-38082224	HepG2	liver:	n/a	chr14:38082041-38082052
13	CEBPB	chr14:38104983-38105178	HepG2	liver:	n/a	chr14:38105134-38105145
14	CEBPB	chr14:38094973-38095262	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:38111175-38111242	H1-hESC	embryonic stem cell:	n/a	chr14:38111183-38111194
16	CEBPB	chr14:38081936-38082182	A549	lung:	n/a	chr14:38082041-38082052
17	CEBPB	chr14:38081873-38082193	IMR90	lung:	n/a	chr14:38082041-38082052
18	CEBPB	chr14:38082000-38082206	K562	blood:	n/a	chr14:38082041-38082052
19	CEBPB	chr14:38111137-38111227	HepG2	liver:	n/a	chr14:38111183-38111194
20	CHD1	chr14:38091509-38091666	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr14:38091494-38092161	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr14:38080203-38080266	HepG2	liver:	n/a	n/a
23	CHD2	chr14:38124722-38124913	K562	blood:	n/a	n/a
24	CTBP2	chr14:38091299-38092266	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr14:38091520-38091670	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr14:38091400-38091550	HPF	lung:	n/a	n/a
27	CTCF	chr14:38091500-38091650	AG10803	skin:	n/a	n/a
28	CTCF	chr14:38080680-38080830	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr14:38080720-38080870	HUVEC	blood vessel:	n/a	n/a
30	CTCF	chr14:38080795-38080801	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr14:38080720-38080870	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr14:38080720-38080870	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr14:38091420-38091570	HCM	heart:	n/a	n/a
34	CTCF	chr14:38091400-38091550	HRE	kidney:	n/a	n/a
35	CTCF	chr14:38091609-38091610	IMR90	lung:	n/a	n/a
36	CTCF	chr14:38091460-38091710	HRE	kidney:	n/a	n/a
37	CTCF	chr14:38091500-38091650	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr14:38091420-38091570	BJ	skin:	n/a	n/a
39	CTCF	chr14:38091440-38091590	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr14:38080740-38080890	HAc	cerebellar:	n/a	n/a
41	CTCF	chr14:38091440-38091590	HFF	foreskin:	n/a	n/a
42	CTCF	chr14:38091480-38091630	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr14:38134905-38134914	GM10248	blood:	n/a	n/a
44	CTCF	chr14:38080560-38080710	NHEK	skin:	n/a	n/a
45	CTCF	chr14:38101576-38101679	Fibrobl	skin:	n/a	n/a
46	CTCF	chr14:38091460-38091610	BJ	skin:	n/a	n/a
47	CTCF	chr14:38091820-38091970	AG04449	skin:	n/a	chr14:38091919-38091932 chr14:38091916-38091934
48	CTCF	chr14:38080640-38080790	NHEK	skin:	n/a	n/a
49	CTCF	chr14:38091460-38091610	AG04449	skin:	n/a	n/a
50	CTCF	chr14:38091460-38091610	AG04450	lung:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:38080446-38080496	HRPEpiC	eye:	n/a
2	chr14:38080446-38080496	HRPEpiC	eye:	n/a
3	chr14:38091926-38091976	AoSMC	blood vessel:	n/a
4	chr14:38119405-38119455	AG09319	gingival:	n/a
5	chr14:38095081-38095131	HCT-116	colon:	n/a
6	chr14:38091824-38091874	NHBE	bronchial:	n/a
7	chr14:38091926-38091976	BE2_C	brain:	n/a
8	chr14:38080446-38080496	NH-A	brain:	n/a
9	chr14:38080904-38080954	BJ	skin:	n/a
10	chr14:38083827-38083877	HEK293	kidney:	embryo
11	chr14:38080048-38080098	HRCEpiC	kidney:	n/a
12	chr14:38087605-38087655	PrEC	prostate:	n/a
13	chr14:38091400-38091450	MCF-7	breast:	n/a
14	chr14:38080314-38080364	MCF-7	breast:	n/a
15	chr14:38091644-38091694	HCT-116	colon:	n/a
16	chr14:38091824-38091874	PFSK-1	brain:	n/a
17	chr14:38080314-38080364	RPTEC	kidney:	n/a
18	chr14:38080048-38080098	LNCaP	prostate:	n/a
19	chr14:38080904-38080954	HPAEpiC	pulmonary alveolar:	n/a
20	chr14:38091644-38091694	NT2-D1	testis:	n/a
21	chr14:38095081-38095131	AoSMC	blood vessel:	n/a
22	chr14:38092080-38092130	HepG2	liver:	n/a
23	chr14:38091824-38091874	GM12878	blood:	n/a
24	chr14:38080904-38080954	GM06990	blood:	n/a
25	chr14:38092845-38092895	AG04449	skin:	fetal
26	chr14:38080904-38080954	AG04450	lung:	fetal
27	chr14:38092845-38092895	ECC-1	luminal epithelium:	n/a
28	chr14:38091926-38091976	HUVEC	blood vessel:	n/a
29	chr14:38087605-38087655	AG09319	gingival:	n/a
30	chr14:38087605-38087655	U87	brain:	n/a
31	chr14:38091400-38091450	Hepatocyte	liver:	n/a
32	chr14:38083827-38083877	Jurkat	blood:	n/a
33	chr14:38087605-38087655	NHBE	bronchial:	n/a
34	chr14:38092175-38092225	Jurkat	blood:	n/a
35	chr14:38080048-38080098	AG04450	lung:	fetal
36	chr14:38095081-38095131	A549	lung:	n/a
37	chr14:38083827-38083877	AoSMC	blood vessel:	n/a
38	chr14:38091824-38091874	LNCaP	prostate:	n/a
39	chr14:38091400-38091450	HL-60	blood:	n/a
40	chr14:38092080-38092130	HCPEpiC	choroid plexus:	n/a
41	chr14:38091644-38091694	NHDF-neo	bronchial:	n/a
42	chr14:38080446-38080496	SAEC	small airway:	n/a
43	chr14:38091644-38091694	Jurkat	blood:	n/a
44	chr14:38092175-38092225	AG09319	gingival:	n/a
45	chr14:38092080-38092130	HMEC	breast:	n/a
46	chr14:38080904-38080954	HRCEpiC	kidney:	n/a
47	chr14:38080314-38080364	Hepatocyte	liver:	n/a
48	chr14:38092175-38092225	HIPEpiC	eye:	n/a
49	chr14:38119405-38119455	HCM	heart:	n/a
50	chr14:38095081-38095131	Caco-2	colon:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:38109867..38112781-chr14:38119992..38121808,2	MCF-7	breast:
2	chr14:38111721..38115535-chr14:38116911..38121515,5	MCF-7	breast:
3	chr14:38060951..38065801-chr14:38133423..38140633,9	MCF-7	breast:
4	chr14:38102182..38104874-chr14:38120835..38123801,2	MCF-7	breast:
5	chr14:38106973..38109198-chr14:38118349..38121005,2	MCF-7	breast:
6	chr14:38120422..38122023-chr14:38122451..38124652,2	MCF-7	breast:
7	chr14:38071630..38073230-chr14:38078352..38080400,2	MCF-7	breast:
8	chr14:38110170..38113216-chr14:38180772..38183600,3	MCF-7	breast:
9	chr14:38039037..38041156-chr14:38111420..38114016,2	MCF-7	breast:
10	chr14:38060700..38073158-chr14:38106984..38130497,55	MCF-7	breast:
11	chr14:38064196..38065060-chr14:38110298..38110849,2	MCF-7	breast:
12	chr14:38061292..38062805-chr14:38087179..38088948,2	MCF-7	breast:
13	chr14:38087054..38090015-chr14:38178315..38180907,2	MCF-7	breast:
14	chr14:37718130..37720442-chr14:38122398..38124870,2	MCF-7	breast:
15	chr14:38052799..38056645-chr14:38110576..38115505,4	MCF-7	breast:
16	chr14:38117406..38120270-chr14:38178890..38183081,3	MCF-7	breast:
17	chr14:38063507..38068018-chr14:38092953..38097909,4	MCF-7	breast:
18	chr14:38135828..38138506-chr14:38180627..38182501,2	MCF-7	breast:
19	chr14:38057805..38059842-chr14:38111890..38113627,2	MCF-7	breast:
20	chr14:38071136..38074087-chr14:38084862..38087700,2	MCF-7	breast:
21	chr14:38063619..38066171-chr14:38084073..38087227,3	MCF-7	breast:
22	chr14:38111721..38115535-chr14:38116911..38121515,5	MCF-7	breast:
23	chr14:38110549..38113085-chr14:38155124..38157508,2	MCF-7	breast:
24	chr14:38060438..38062133-chr14:38130712..38132708,2	MCF-7	breast:
25	chr14:38065961..38068630-chr14:38077390..38079134,2	K562	blood:
26	chr14:38061711..38062291-chr14:38118987..38119728,2	MCF-7	breast:
27	chr14:38121505..38124400-chr14:38179462..38181983,2	MCF-7	breast:
28	chr14:38137638..38140285-chr14:38157919..38160073,2	MCF-7	breast:
29	chr14:38101094..38102983-chr14:38112634..38114320,2	MCF-7	breast:
30	chr14:38056260..38058013-chr14:38136356..38140465,3	MCF-7	breast:
31	chr14:38108926..38110545-chr14:38112371..38115068,2	MCF-7	breast:
32	chr14:38120422..38122023-chr14:38122451..38124652,2	MCF-7	breast:
33	chr14:38101094..38102983-chr14:38112634..38114320,2	MCF-7	breast:
34	chr14:38109867..38112781-chr14:38119992..38121808,2	MCF-7	breast:
35	chr14:38137632..38140312-chr14:38141019..38143766,2	MCF-7	breast:
36	chr14:38063388..38066234-chr14:38126834..38129213,3	MCF-7	breast:
37	chr14:38065320..38065829-chr14:38119737..38120477,2	MCF-7	breast:
38	chr14:38106973..38109198-chr14:38118349..38121005,2	MCF-7	breast:
39	chr14:38053183..38055954-chr14:38113662..38116528,3	MCF-7	breast:
40	chr14:38060301..38063769-chr14:38137094..38139893,4	MCF-7	breast:
41	chr14:38050621..38053581-chr14:38135495..38137848,2	MCF-7	breast:
42	chr14:38108926..38110545-chr14:38112371..38115068,2	MCF-7	breast:
43	chr14:38102182..38104874-chr14:38120835..38123801,2	MCF-7	breast:
44	chr14:38072737..38074594-chr14:38109298..38110859,2	MCF-7	breast:
45	chr14:38060550..38070653-chr14:38108679..38125791,47	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MIPOL1-3	chr14:38092102-38092208	XLOC_010806

No data

Variant related genes	Relation type
TTC6	TF binding region
TTC6	CpG island
ENSG00000129514	chromatin interactions
ENSG00000139865	chromatin interactions

Extended variants
information (count: 2094 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2094 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536508667	chr14:38078044-38078045	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs532773638	chr14:38078062-38078063	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs533718991	chr14:38078067-38078068	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs564707545	chr14:38078076-38078077	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs7150507	chr14:38078098-38078099	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs567407236	chr14:38078109-38078110	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs71405800	chr14:38078115-38078116	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs555795636	chr14:38078173-38078174	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs139909336	chr14:38078186-38078187	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs544703815	chr14:38078239-38078240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558313337	chr14:38078326-38078327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145362406	chr14:38078376-38078377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537179855	chr14:38078378-38078379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560748927	chr14:38078464-38078465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs34273412	chr14:38078490-38078491	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs191915909	chr14:38078543-38078544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7151000	chr14:38078588-38078589	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs113084503	chr14:38078604-38078605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546177686	chr14:38078618-38078619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7151179	chr14:38078640-38078641	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs527389613	chr14:38078663-38078664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149840842	chr14:38078706-38078707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567500983	chr14:38078708-38078709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536541357	chr14:38078748-38078749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559457001	chr14:38078767-38078768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs116671509	chr14:38078802-38078803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538215899	chr14:38078857-38078858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs34108211	chr14:38078861-38078862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533624280	chr14:38078889-38078890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs578005450	chr14:38078899-38078900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574798791	chr14:38078915-38078916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs74045683	chr14:38078938-38078939	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs377751174	chr14:38078960-38078961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554072967	chr14:38079011-38079012	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574208641	chr14:38079044-38079045	Strong transcription Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs542889031	chr14:38079051-38079052	Strong transcription Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs35143297	chr14:38079065-38079066	Strong transcription Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs72674258	chr14:38079126-38079127	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544563298	chr14:38079157-38079158	Strong transcription Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564899264	chr14:38079236-38079237	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186644265	chr14:38079244-38079245	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189879990	chr14:38079251-38079252	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560897136	chr14:38079324-38079325	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376231262	chr14:38079328-38079329	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370331442	chr14:38079352-38079353	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117841252	chr14:38079461-38079462	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550014549	chr14:38079497-38079498	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182397866	chr14:38079511-38079512	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530502868	chr14:38079617-38079618	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145834694	chr14:38079708-38079709	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38073000-38080200	Weak transcription	Gastric	stomach
2	chr14:38073400-38079000	Weak transcription	Liver	Liver
3	chr14:38077200-38078400	Enhancers	HepG2	liver
4	chr14:38078400-38078800	Weak transcription	HepG2	liver
5	chr14:38078800-38080800	Strong transcription	HepG2	liver
6	chr14:38079000-38079200	Bivalent Enhancer	Fetal Kidney	kidney
7	chr14:38079000-38080200	Strong transcription	Liver	Liver
8	chr14:38079800-38080000	Flanking Bivalent TSS/Enh	Fetal Lung	lung
9	chr14:38079800-38080600	Bivalent Enhancer	Fetal Brain Male	brain
10	chr14:38080000-38080200	Bivalent/Poised TSS	Fetal Brain Female	brain
11	chr14:38080000-38080200	Bivalent Enhancer	Fetal Stomach	stomach
12	chr14:38080000-38080800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
13	chr14:38080000-38080800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
14	chr14:38080000-38081000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
15	chr14:38080200-38080400	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr14:38080200-38080400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr14:38080200-38080400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr14:38080200-38080400	Bivalent/Poised TSS	HMEC	breast
19	chr14:38080200-38080400	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
20	chr14:38080200-38080600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr14:38080200-38080600	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr14:38080200-38080600	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr14:38080200-38080600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:38080200-38080600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
25	chr14:38080200-38080600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
26	chr14:38080200-38080600	Bivalent/Poised TSS	NH-A	brain
27	chr14:38080200-38080800	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr14:38080200-38080800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
29	chr14:38080200-38080800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr14:38080200-38080800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
31	chr14:38080200-38080800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:38080200-38080800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr14:38080200-38080800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
34	chr14:38080200-38080800	Bivalent/Poised TSS	NHEK	skin
35	chr14:38080200-38081000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr14:38080200-38081000	ZNF genes & repeats	Gastric	stomach
37	chr14:38080200-38081200	Bivalent/Poised TSS	Brain Anterior Caudate	brain
38	chr14:38080200-38081400	Weak transcription	Liver	Liver
39	chr14:38080200-38084400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:38080400-38080600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr14:38080400-38080600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr14:38080400-38080600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr14:38080400-38080600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
44	chr14:38080400-38080600	Flanking Bivalent TSS/Enh	HMEC	breast
45	chr14:38080400-38080600	Bivalent/Poised TSS	HUVEC	blood vessel
46	chr14:38080400-38080800	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr14:38080600-38080800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
48	chr14:38080600-38080800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr14:38080600-38080800	Bivalent Enhancer	Adipose Nuclei	Adipose
50	chr14:38080600-38080800	Bivalent/Poised TSS	Brain Germinal Matrix	brain

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